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US2359310A - Chemical process - Google Patents

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US2359310A
US2359310A US379398A US37939841A US2359310A US 2359310 A US2359310 A US 2359310A US 379398 A US379398 A US 379398A US 37939841 A US37939841 A US 37939841A US 2359310 A US2359310 A US 2359310A
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catalyst
reaction zone
vapors
solid
powdered
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US379398A
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Charles E Hemminger
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Standard Oil Development Co
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Standard Oil Development Co
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/18Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
    • B01J8/1845Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles with particles moving upwards while fluidised

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  • present invention relates to a process and apparatus for carrying the process into effect for treating hydrocarbon oils, and more particularly it relates to improvements. in the continuous Y cracking of hydrocarbon oils in a process where the powdered catalyst is suspended in the vapors during the reaction.
  • the hydrocarbon oil contains the catalyst suspended therein during thev reaction.
  • the cold oil is vaporized and preheated to say a temperature of 825-950 F., and the catalyst' having a particle size of from about -80 microns issuspended inthe vapors either before or after they are heated to the temperature indicated, and the reaction is then allowed to take place in'a reaction zone which is ordinarily of the form of a cylindrical retort or a conical retort.
  • the catalyst may or may not be resident in the catalyst zone for the same period of time as do all portions thereof. 4For example, in a reactor of the type described, the ilow of vapors containing catalyst is usually upward and its vlinear velocity is rather low, often being from 1-3 ft.
  • reaction zone This is a situation where the reaction zone is a hollow vessel and the path of the suspension is unobstructed within the reaction zone.
  • the eect of the bailies. together with the sidewalls, is to provide the-.equivalent of a plurality of pipes of relatively small diameter, say 3-5' inches, disposed inv parallel.
  • mixing.of the catalyst from the top of the reactor to the bottom in eddy currents is prevented by the bailles which prevent or limit the eddy currents in the reactor, slippage of the gas and the particles exists. Consequently, by regulating thevelocity from 1-5 feet per second, the' diilerential times of contact of the catalyst and vapors canbe var. ed at will. This being the case, it is possible to control the contact time between vapors and catalyst inthe reactor by regulating the linear velocity of the suspension.
  • the reaction vapors pass upno part of. the present invention and these may be carried out according to any conventional method.
  • Perforated tube sheets 32 and 33 may be the terminals of a plurality of pipes or flues so disposed and arranged as to effect parallel flow o! the iiuid therethrough.
  • an arrangement may be employed which is similar to the well-known ilre tube steel boiler.
  • the headers are tube sheets 32 and 33,
  • the bailles need not be continuous but may be intermittent along the height to allow mixing from side to side to equalize pressures. This may be done by holes in the baboards or even using oiIset bafiies not in line with one another.
  • the improvement which comprises subdividing the stream of powdered catalyst and hydrocarbon vapor into a plurality of separate streams for at least part of the height of said reaction zone to limit undesirable mixing and eddy currents and to have the time of residence of the powdered catalyst in the subdivided streams in said reaction zone substantially the same while at the same time maintaining a relatively low vapor velocity to permit some settling of the 'catalyst resulting in relatively high concentration of catalyst in the vapors in the sepatively large cross section and wherein the velocity of the gaseous fluid is relatively low and due to slippage or settling of the solid the concentration of the solid in theupflowing gaseous fluid is relatively high and eddy currents are formed causing desirable and undesirable mixing of the solid and gaseous uid, the improvement which comprises subdividing the stream of solid and gaseous fluid into a plurality of streams for

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)

Description

Oct. 3, 1944.
c. E. HEMMINGER 2,359,310
CHEMICAL PROCESS Filed Feb. 18, 1941 CA rALYs r AND VA7N 12S Oc/TLET VA 'POP S /A/LEY' cnvwan /VON OOM'PRESS/o/v SCREW FEED l ZEAQTOR Patentedl Oct. 3, 1944 FFicE'- CHEMICAL PROCESS Charles E. Hemmlnger, Westileld, N. J., assigner to Standard Oil porationv of Delaware Application February 1s, 194,1, serial No. 379,398
i (ci. 19e- 5- z) 10 Claims.
present invention relates to a process and apparatus for carrying the process into effect for treating hydrocarbon oils, and more particularly it relates to improvements. in the continuous Y cracking of hydrocarbon oils in a process where the powdered catalyst is suspended in the vapors during the reaction.
In the type of process which is herein described t and claimed, the hydrocarbon oil contains the catalyst suspended therein during thev reaction.
The cold oil is vaporized and preheated to say a temperature of 825-950 F., and the catalyst' having a particle size of from about -80 microns issuspended inthe vapors either before or after they are heated to the temperature indicated, and the reaction is then allowed to take place in'a reaction zone which is ordinarily of the form of a cylindrical retort or a conical retort. In the'case where the retort is substantially cylindrical, the catalyst may or may not be resident in the catalyst zone for the same period of time as do all portions thereof. 4For example, in a reactor of the type described, the ilow of vapors containing catalyst is usually upward and its vlinear velocity is rather low, often being from 1-3 ft. per second. Where the vapors contain 10-20 lbs. of catalyst per cubic foot, a considerable amount of slippage or settling may take place as to some portions oi' the catalyst whereas other portions remain in the catalytic zone `for arelatively short period ottime. In other words, let us suppose that the average time of residence of the catalyst in the zone is ten seconds. It may be and often is the fact that a substantial portion ofy that catalyst,
which is fresh or regenerated catalyst, remains in the reaction zone for a period-of less than tive seconds. It apparently passes straight through .l
` the reaction zone. This is a situation where the reaction zone is a hollow vessel and the path of the suspension is unobstructed within the reaction zone. e
I have devised a method and apparatus for correcting the above deficiency in prior reactors. and I accomplish this result by means of bailles disposed within the reactor, which battles cause the suspension to flow through the reaction zone in parallel or conned streams, and by this means I effect the result of preventing undue mixing and insure substantially equal time oi' residence of all particles of catalyst in the reaction zone.
My invention will be best understood by reference to the accompanying drawing, in which Fig-v ure I shows a' vertical elevation partly in section oi' my improved reactor, and Figure II is a crosslsection taken along the line II-lI of .Figure I.
' -The prevention of mixing in a reactor is desiry Development Company, 'a cor- 1 lalumina silica or magnesia silica compositions, is
discharged from hopper Il into the casing of screw conveyor I8,- which conveyor is preferably of the non-compression type. The conveyor discharges the powdered material into the bottom of conduit Ii. where it becomes dispersed in the oil vapors also entering I2, and the dispersion then is forced upwardly through reactor 20 which reactor carries a plurality of baille plates 28 which baule plates, together with the inner walls of the reactor, forma plurality of cells or conduits through which the vapors ascend. Distributor plates 2l distribute the flowequally to the various tubes or sectors. It is believed to be obvious that the conduits and the distributor plates reduce the tendency of the catalyst to intermix (i. e., from top to bottom) within the reactor and the net eiect is that the suspension passes upwardly in a plurality of parallel or confined streams of reduced cross-section. The eect of the bailies. together with the sidewalls, is to provide the-.equivalent of a plurality of pipes of relatively small diameter, say 3-5' inches, disposed inv parallel. Although mixing.of the catalyst from the top of the reactor to the bottom in eddy currents is prevented by the bailles which prevent or limit the eddy currents in the reactor, slippage of the gas and the particles exists. Consequently, by regulating thevelocity from 1-5 feet per second, the' diilerential times of contact of the catalyst and vapors canbe var. ed at will. This being the case, it is possible to control the contact time between vapors and catalyst inthe reactor by regulating the linear velocity of the suspension. The reaction vapors pass upno part of. the present invention and these may be carried out according to any conventional method.
able because it has been found that in cracking of gas oil the amount of carbon on the catalyst in the initial stages of cracking iniluences the carbon formation. In case the carbon on the inlet catalyst is 1%v and that on the outlet is 3%, if mixing is allowed. the average concentration is the same as the outlet, 3%, and almost all the cracking is carried out in the presence of 3% carbon. However, if mixing is prevented, part of the cracking'will be with catalyst of 1% carbon and part with catalyst of 2% carbon. This reduction in carbon on catalyst during cracking is suiiicient to decrease the carbon formation by 'from 25 to 50% for the gasoline formation.
Many modifications oi the present invention may be made by those skilled in the art without departing from the spirit thereof. Perforated tube sheets 32 and 33 may be the terminals of a plurality of pipes or flues so disposed and arranged as to effect parallel flow o! the iiuid therethrough. For instance, an arrangement may be employed which is similar to the weil-known ilre tube steel boiler. Of course, it will be understood that the headers are tube sheets 32 and 33,
- are imperforate except at the respective ends of the conduits 34 where they are necessarily perforated and correspond in diameter and crossf section of chamber or cells as illustrated but they may take any form. Also. the bailles need not be continuous but may be intermittent along the height to allow mixing from side to side to equalize pressures. This may be done by holes in the baiiles or even using oiIset bafiies not in line with one another.
What I claim is:
l. In the continuous contacting of vapors with solid catalytic materials in a process wherein -the solid catalyst in powdered form is suspended in hot vapors during a reaction, the improvement which comprises forcing the hot vapors containing solid catalyst suspended therein into a reaction zone. causing the hot vapors and solid to ilow upwardly through the reaction zone in a plurality of parallel confined streams of relatively small cross-sectional area separated only by vertical partitions and withdrawing the reaction products from the top of the reaction zone, the process being characterized by the feature that during the passage of the suspension through the reaction zone the velocity of the vapors is maintained low and due to slippage or settling of the catalyst the concentration of the catalyst in the vapors in the separate streams is relatively high to give the desired time of contact between the vapors and catalyst while at the same time limiting eddy currents and undesirable mixing in said reaction zone which would be obtained if an unobstructed reaction zone Iwere used.
2. The process set forth in claim l 'in which the solid material is a powdered cracking catalyst and the vapors are hydrocarbons boiling substantially within the gas oil range.
3. The process set forth in claim 1 in which the velocity of the vapors passing through the reaction zone is from 1 to 5 feet per second.
. 4. The process set forth in claim 1 in which the solid catalyst is a hydrocarbon conversion catalyst and the vapors are hydrocarbons in a gaseous state.
5. A process as set forth in claim 1 wherein the suspension passing through said reaction zone as a plurality of confined streams has a relatively large density and the vapors contain about to pounds of catalyst per cubic foot.
6. In a process wherein the catalytic conversion of hydrocarbons is carried out by passing a. stream of powdered catalyst suspended in a hydrocarbon assas'io divide said zone into a plurality of vertical passageways so that the powdered catalyst and hydrocarbon pass upwardly through said reaction mne in a plurality of 'streams and under conditions to obtain settling of the catalyst in the gaseous hydrocarbon and to obtain relatively ,high concentration voi! catalyst in the gaseous hydrocarbon in -the streams and the time of residence of allofthe powdered catalyst in the plurality of streams in said reaction zone is substantially thef'same and undesirable mixing of the catalyst from the top of said reaction zone to the bottom thereof caused by 'eddy currents is limited and less carbonaceous material is deposited on the powdered catalyst per volume of the reaction product produced than if the enlarged reaction zone were used without the partitions.
7. In a process wherein the catalytic conversion of hydrocarbons is carried out by passing a stream of powdered catalyst suspended in a hydrocarbon in a gaseous state under reaction conditions upwardly in a vertically arranged reaction zone having a relatively large cross section and wherein the velocity of the gaseous hydrocarbon is maintained low and due to slippage or settling of the catalyst relativeLv high concentration of catalyst in hydrocarbon is obtained and wherein eddy currents are formed and undesirable mixing is obtained and a relatively largeamount of solid carbonaceous material is depositedA on the catalyst particles per volume of gasoline produced when an unobstructed reaction zone is used, the improvement which comprises subdividing said reaction zone into a plurality of vertical cells whereby undesirable mixing of the catalyst in said reaction zone caused 4 by eddy currents is limited and less solid carbonaceous material is deposited on the catalyst particles per volume of gasoline produced during the conversion than if the enlarged reaction zone were used without the cells.
8. In a process wherein the catalytic conversion of hydrocarbons is carried out in the presence of powdered catalyst by passing a. stream of powdered catalyst suspended in hydrocarbon vapors under reaction conditions upwardly in a vertically arranged reaction zone having a relatively large cross section and wherein the velocity of the vapors in said reaction zone is relatively low and due to slippage or settling o! the catalyst the concentration of catalyst in the upowing vapors in said reaction zone is relatively high and eddy currents are formed causing desirable and undesirable mixing of the catalyst in said reaction zone, the improvement which comprises subdividing the stream of powdered catalyst and hydrocarbon vapor into a plurality of separate streams for at least part of the height of said reaction zone to limit undesirable mixing and eddy currents and to have the time of residence of the powdered catalyst in the subdivided streams in said reaction zone substantially the same while at the same time maintaining a relatively low vapor velocity to permit some settling of the 'catalyst resulting in relatively high concentration of catalyst in the vapors in the sepatively large cross section and wherein the velocity of the gaseous fluid is relatively low and due to slippage or settling of the solid the concentration of the solid in theupflowing gaseous fluid is relatively high and eddy currents are formed causing desirable and undesirable mixing of the solid and gaseous uid, the improvement which comprises subdividing the stream of solid and gaseous fluid into a plurality of streams for at least part of the height of said reaction zone to limit undesirable mixing and eddy currents While maintaining a relatively low velocity of the gaseous fluid to permit some settling of the solid resulting in relatively high concentration of the solid in the gaseous fluid in the separate streams to give the desired time of contact between the solid and gaseous fluid.
10. In a process wherein gaseous fluid is contacted with a powdered contact solid by passing powdered solid and a gaseous fluid under reaction conditions into a vertically arranged reaction zone having a relatively large cross section and wherein the gaseous fluid flows upwardly through said reaction zone and wherein the velocity of the gaseous fluid is relatively low and due to slippage or settling of the'solid the concentration of the solid in the upflowing gaseous fluid is relatively high and eddy currents are formed causing desirable and undesirable mixing of the solid and gaseous fluid, the improvement which comprises subdividing the reaction zone into a fplurality of vertical cells so that the gaseous fluid is subdivided into a plurality of streams for at least part of the height of said reaction zone to limit undesirable mixing and eddy currents while maintaining a relatively 10W .velocity of the gaseous fluid to permit some settling of the solid resulting in relatively high concentration of the solid in the gaseous iluid in the separate streams to give the desired time of contact between .the l solid and gaseous fluid.
^ CHARLES E. HEMMINGER.
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Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2422262A (en) * 1944-08-02 1947-06-17 Standard Oil Dev Co Apparatus for contacting solid particles with gaseous fluids
US2455561A (en) * 1946-06-28 1948-12-07 Kellogg M W Co Reducing disengaging height in fluidized powder systems
US2457098A (en) * 1943-07-29 1948-12-21 Socony Vacuum Oil Co Inc Apparatus for conducting reactions in the presence of a contact mass
US2472502A (en) * 1945-07-28 1949-06-07 Standard Oil Dev Co Apparatus for stripping finely dividfd solids
US2481439A (en) * 1945-08-07 1949-09-06 Standard Oil Dev Co Gas-solids contacting apparatus including means for stripping solid particles
US2491536A (en) * 1945-08-21 1949-12-20 Standard Oil Dev Co Gas-solid contacting apparatus, including means for stripping solid particles
US2545165A (en) * 1945-08-14 1951-03-13 Standard Oil Dev Co Gas-solid contacting apparatus, including means for stripping solid particles
US2626289A (en) * 1950-03-30 1953-01-20 Standard Oil Dev Co Process for polymerization in the presence of a fluid solid polymerization catalyst
US2641450A (en) * 1946-10-19 1953-06-09 Hydrocarbon Research Inc Method of transferring heat by a powdered thermophore in a state of dense phase fluidization
US2681273A (en) * 1947-08-23 1954-06-15 Standard Oil Dev Co Process for making combustible gas
US2683657A (en) * 1948-05-29 1954-07-13 Hydrocarbon Research Inc Gasification of carbonaceous solids
US2760842A (en) * 1952-03-03 1956-08-28 Gulf Research Development Co Fluidized fixed bed process and apparatus
US2769771A (en) * 1952-12-10 1956-11-06 Exxon Research Engineering Co Contacting of gases with fluidized solids with the use of chains in the fluidized bed
US2853369A (en) * 1955-01-12 1958-09-23 Kolbel Herbert Apparatus for carrying out gaseous catalytic reactions in liquid medium
US3113095A (en) * 1960-05-17 1963-12-03 Raphael M Braca Transport reactors
US3889042A (en) * 1972-12-26 1975-06-10 Allied Chem Method and apparatus for cooling and insulating electrical equipment
US4316792A (en) * 1979-12-21 1982-02-23 The Lummus Company Hydroliquefaction of coal

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2457098A (en) * 1943-07-29 1948-12-21 Socony Vacuum Oil Co Inc Apparatus for conducting reactions in the presence of a contact mass
US2422262A (en) * 1944-08-02 1947-06-17 Standard Oil Dev Co Apparatus for contacting solid particles with gaseous fluids
US2472502A (en) * 1945-07-28 1949-06-07 Standard Oil Dev Co Apparatus for stripping finely dividfd solids
US2481439A (en) * 1945-08-07 1949-09-06 Standard Oil Dev Co Gas-solids contacting apparatus including means for stripping solid particles
US2545165A (en) * 1945-08-14 1951-03-13 Standard Oil Dev Co Gas-solid contacting apparatus, including means for stripping solid particles
US2491536A (en) * 1945-08-21 1949-12-20 Standard Oil Dev Co Gas-solid contacting apparatus, including means for stripping solid particles
US2455561A (en) * 1946-06-28 1948-12-07 Kellogg M W Co Reducing disengaging height in fluidized powder systems
US2641450A (en) * 1946-10-19 1953-06-09 Hydrocarbon Research Inc Method of transferring heat by a powdered thermophore in a state of dense phase fluidization
US2681273A (en) * 1947-08-23 1954-06-15 Standard Oil Dev Co Process for making combustible gas
US2683657A (en) * 1948-05-29 1954-07-13 Hydrocarbon Research Inc Gasification of carbonaceous solids
US2626289A (en) * 1950-03-30 1953-01-20 Standard Oil Dev Co Process for polymerization in the presence of a fluid solid polymerization catalyst
US2760842A (en) * 1952-03-03 1956-08-28 Gulf Research Development Co Fluidized fixed bed process and apparatus
US2769771A (en) * 1952-12-10 1956-11-06 Exxon Research Engineering Co Contacting of gases with fluidized solids with the use of chains in the fluidized bed
US2853369A (en) * 1955-01-12 1958-09-23 Kolbel Herbert Apparatus for carrying out gaseous catalytic reactions in liquid medium
US3113095A (en) * 1960-05-17 1963-12-03 Raphael M Braca Transport reactors
US3889042A (en) * 1972-12-26 1975-06-10 Allied Chem Method and apparatus for cooling and insulating electrical equipment
US4316792A (en) * 1979-12-21 1982-02-23 The Lummus Company Hydroliquefaction of coal

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